Scientific name	Authority	First published in
Ledum latifolium	Jacq.	Collectanea 2: 308 (1789)
Ledum pacificum	Small	N. Amer. Fl. 29: 37 (1914)
Ledum canadense	G.Lodd.	Bot. Cab. 11: t. 1049 (1826)
Ledum groenlandicum	Oeder	Fl. Dan. 4(10): 5 (1771)
Ledum palustre subsp. groenlandicum	(Oeder) Rosenv.	Acta Univ. Lund., 2 , 44(1): 1219 (1948)
Ledum groenlandicum var. aridiphilum	D Löve	Taxon 17: 89 (1968)
Ledum latifolium var. canadense	(Lodd.) DC.	Prodr. 7: 730 (1839)
Ledum palustre var. latifolium	(Jacq.) Hook.	Fl. Bor.-Amer. 2: 44 (1834)
Ledum palustre var. groenlandicum	(Oeder) Rosenv.	Meddel. Grønland 3:692. (1892)

Common names Top

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Filter by language:

Language	Common/alternative name
English	common labrador tea
atj	wisakipok
Bulgarian	гренландски рододендрон
cr	mirowepok
Danish	grønlandsk post
German	ledum groenlandicum
German	grönländischer porst
French	thé du labrador
French	lédon du groenland
French	lédon du groënland
French	ledum groenlandicum
French	the du labrador
Icelandic	heiðaflóki
Japanese	アカゲノイソツツジ
kl	qajaasaq
kl	qajaasat
Dutch	moerasrozemarijn
Russian	Рододендрон гренландский
Russian	Багульник гренландский
Russian	ledum groenlandicum
Swedish	bredbladig skvattram
Turkish	ledum groenlandicum
Turkish	labradorçayı

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

Alternate between 20°C and 4°C for 3 months each, across multiple cycles, acknowledging that germination may be prolonged.

Requires Light or Surface Sowing: These seeds need light to germinate and should not be covered with soil or only very lightly. They are often very small and sown directly on the surface of the growing medium.

peat based medium

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- Eastern Asia
  - Japan

Europe click to expand
- Middle Europe
  - Germany
- Northern Europe
  - Great Britain

Northern America click to expand
- Eastern Canada
  - Labrador
  - New Brunswick
  - Newfoundland
  - Nova Scotia
  - Ontario
  - Prince Edward Island
  - Québec
- North-central U.S.A.
  - Minnesota
  - Wisconsin
- Northeastern U.S.A.
  - Connecticut
  - Maine
  - Massachusetts
  - Michigan
  - New Hampshire
  - New York
  - Pennsylvania
  - Vermont
- Northwestern U.S.A.
  - Idaho
  - Oregon
  - Washington
- Subarctic America
  - Alaska
  - Greenland
  - Northwest Territorie
  - Nunavut
  - Yukon
- Western Canada
  - Alberta
  - British Columbia
  - Manitoba
  - Saskatchewan

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001279386
UNII	U16KIM2T9T
Canadensys	5557
Tropicos	50303842
INPN	762052
KEW	urn:lsid:ipni.org:names:284230-2
The Plant List	tro-50303842
Open Tree Of Life	649881
Observations.org	436608
NCBI Taxonomy	49605
IPNI	284230-2
iNaturalist	180413
GBIF	2882984
Freebase	/m/08x1bk
WisFlora	13261
Elurikkus	323852
USDA GRIN	417158
Wikipedia	Rhododendron_groenlandicum

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

Phytochemical Profiling and Biological Activities of Rhododendron Subsect. Ledum: Discovering the Medicinal Potential of Labrador Tea Species in the Northern Hemisphere

Vengrytė M, Raudonė L

Plants (Basel)

21-Mar-2024

PMCID:	PMC10975282
doi:	10.3390/plants13060901
PMID:	38592945

Shading contributes to Sphagnum decline in response to warming

Norby RJ, Baxter T, Živković T, Weston DJ

Ecol Evol

19-Sep-2023

PMCID:	PMC10507575
doi:	10.1002/ece3.10542
PMID:	37732286

Nanoparticle-mediated amelioration of drought stress in plants: a systematic review

Chandrashekar HK, Singh G, Kaniyassery A, Thorat SA, Nayak R, Murali TS, Muthusamy A

3 Biotech

08-Sep-2023

PMCID:	PMC10491566
doi:	10.1007/s13205-023-03751-4
PMID:	37693636

New Plants, New Resources, New Knowledge: Early Introductions of Exotic Plants to Indigenous Territories in Northwestern North America

Turner NJ

Plants (Basel)

28-Aug-2023

PMCID:	PMC10490097
doi:	10.3390/plants12173087
PMID:	37687334

Boreal conifers maintain carbon uptake with warming despite failure to track optimal temperatures

Dusenge ME, Warren JM, Reich PB, Ward EJ, Murphy BK, Stefanski A, Bermudez R, Cruz M, McLennan DA, King AW, Montgomery RA, Hanson PJ, Way DA

Nat Commun

03-Aug-2023

PMCID:	PMC10400668
doi:	10.1038/s41467-023-40248-3
PMID:	37537190

Using long‐term data from a whole ecosystem warming experiment to identify best spring and autumn phenology models

Schädel C, Seyednasrollah B, Hanson PJ, Hufkens K, Pearson KJ, Warren JM, Richardson AD

Plant Environ Interact

29-Jun-2023

PMCID:	PMC10423976
doi:	10.1002/pei3.10118
PMID:	37583877

Role of natural products and intestinal flora on type 2 diabetes mellitus treatment

Aydin OC, Aydın S, Barun S

World J Clin Cases

06-Jan-2023

PMCID:	PMC9846977
doi:	10.12998/wjcc.v11.i1.65
PMID:	36687192

A systematic analysis of anti-diabetic medicinal plants from cells to clinical trials

Omale S, Amagon KI, Johnson TO, Bremner SK, Gould GW

PeerJ

05-Jan-2023

PMCID:	PMC9826616
doi:	10.7717/peerj.14639
PMID:	36627919

Utilization of Indole Acetic Acid with Leucadendron rubrum and Rhododendron pulchrum for the Phytoremediation of Heavy Metals in the Artificial Soil Made of Municipal Sewage Sludge

Chen X, Feng J, Mou H, Liang Z, Ding T, Chen S, Li F

Toxics

31-Dec-2022

PMCID:	PMC9864706
doi:	10.3390/toxics11010043
PMID:	36668769

Revisiting Periodontal Disease in Dogs: How to Manage This New Old Problem?

Cunha E, Tavares L, Oliveira M

Antibiotics (Basel)

01-Dec-2022

PMCID:	PMC9774197
doi:	10.3390/antibiotics11121729
PMID:	36551385

Ericoid mycorrhizal fungi as biostimulants for improving propagation and production of ericaceous plants

Wei X, Zhang W, Zulfiqar F, Zhang C, Chen J

Front Plant Sci

16-Nov-2022

PMCID:	PMC9709444
doi:	10.3389/fpls.2022.1027390
PMID:	36466284

Transcription factor NRF2 as potential therapeutic target for preventing muscle wasting in aging chronic kidney disease patients

Gómez-García EF, del Campo FM, Cortés-Sanabria L, Mendoza-Carrera F, Avesani CM, Stenvinkel P, Lindholm B, Cueto-Manzano AM

J Nephrol

02-Nov-2022

PMCID:	PMC9700608
doi:	10.1007/s40620-022-01484-w
PMID:	36322291

Scale‐dependent effects of marine subsidies on the island biogeographic patterns of plants

Obrist DS, Fitzpatrick OT, Brown NE, Hanly PJ, Nijland W, Reshitnyk LY, Wickham SB, Darimont CT, Reynolds JD, Starzomski BM

Ecol Evol

09-Sep-2022

PMCID:	PMC9461347
doi:	10.1002/ece3.9270
PMID:	36177118

Cryocampsis: a biophysical freeze-bending response of shrubs and trees under snow loads

Ray PM, Bret-Harte MS

PNAS Nexus

25-Jul-2022

PMCID:	PMC9802243
doi:	10.1093/pnasnexus/pgac131
PMID:	36714826

Thermodynamic basis for the demarcation of Arctic and alpine treelines

Martin MR, Kumar P, Sonnentag O, Marsh P

Sci Rep

22-Jul-2022

PMCID:	PMC9307831
doi:	10.1038/s41598-022-16462-2
PMID:	35869102

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
3,7-Dimethylocta-2,6-dienyl acetate	7780	Click to see CC(=CCCC(=CCOC(=O)C)C)C	196.29	unknown	https://doi.org/10.1007/BF00579758
3,7-Dimethylocta-2,6-dienyl formate	7779	Click to see CC(=CCCC(=CCOC=O)C)C	182.26	unknown	https://doi.org/10.1246/NIKKASHI1921.64.1041
Geranyl acetate	1549026	Click to see CC(=CCCC(=CCOC(=O)C)C)C	196.29	unknown	https://doi.org/10.1007/BF00579758 https://doi.org/10.1007/BF00937609
Geranyl formate	5282109	Click to see CC(=CCCC(=CCOC=O)C)C	182.26	unknown	https://doi.org/10.1246/NIKKASHI1921.64.1041
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(3R,5E)-2,6-dimethylocta-1,5,7-trien-3-ol	92256191	Click to see CC(=C)C(CC=C(C)C=C)O	152.23	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.27-0551 https://doi.org/10.1007/BF00566074
3,7-Dimethyl-2,6-octadien-1-ol	4458	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1007/BF00579758
6-Methyl-2-methyleneocta-5,7-dien-3-ol	119847	Click to see CC(=C)C(CC=C(C)C=C)O	152.23	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.27-0551 https://doi.org/10.1007/BF00566074
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1007/BF00579758
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	https://doi.org/10.1007/BF00566074 https://doi.org/10.1007/BF00565890 https://doi.org/10.1007/BF01134621
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	https://doi.org/10.1246/NIKKASHI1921.64.1041 https://doi.org/10.1007/BF00937609
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+)-Bornyl acetate	6950274	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	https://doi.org/10.1007/BF00579758
(1S,2R,5S)-5-propan-2-ylbicyclo[3.1.0]hex-3-ene-2-carbaldehyde	162900349	Click to see CC(C)C12CC1C(C=C2)C=O	150.22	unknown	https://doi.org/10.1007/BF00601281
5-Isopropylbicyclo[3.1.0]hex-2-ene-2-carbaldehyde	530411	Click to see CC(C)C12CC=C(C1C2)C=O	150.22	unknown	https://doi.org/10.1007/BF00601281
5-Propan-2-ylbicyclo[3.1.0]hex-3-ene-2-carbaldehyde	6429043	Click to see CC(C)C12CC1C(C=C2)C=O	150.22	unknown	https://doi.org/10.1007/BF00601281
Bornyl acetate	6448	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	https://doi.org/10.1007/BF00579758
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-trans-Carveol	94221	Click to see CC1=CCC(CC1O)C(=C)C	152.23	unknown	https://doi.org/10.1007/BF00579758
(1R,3S,4S)-3,4-bis(ethenyl)-4-methyl-1-prop-1-en-2-ylcyclohexan-1-ol	162996232	Click to see CC(=C)C1(CCC(C(C1)C=C)(C)C=C)O	206.32	unknown	https://doi.org/10.1007/BF00629824
(2S,4R)-p-Mentha-1(7),8-dien-2-ol	527427	Click to see CC(=C)C1CCC(=C)C(C1)O	152.23	unknown	https://doi.org/10.1007/BF00579758
3-Cyclohexene-1-methanol, alpha,alpha,4-trimethyl-, 1-acetate, (1R)-	11469649	Click to see CC1=CCC(CC1)C(C)(C)OC(=O)C	196.29	unknown	https://doi.org/10.1007/BF00579758
3,4-Bis(ethenyl)-4-methyl-1-prop-1-en-2-ylcyclohexan-1-ol	85650599	Click to see CC(=C)C1(CCC(C(C1)C=C)(C)C=C)O	206.32	unknown	https://doi.org/10.1007/BF00629824
alpha-PHELLANDRENE, (-)-	442482	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	https://doi.org/10.1002/JPS.3080230706
alpha-Terpinyl acetate	111037	Click to see CC1=CCC(CC1)C(C)(C)OC(=O)C	196.29	unknown	https://doi.org/10.1007/BF00579758
Carveol	7438	Click to see CC1=CCC(CC1O)C(=C)C	152.23	unknown	https://doi.org/10.1007/BF00579758
Carvone, (-)-	439570	Click to see CC1=CCC(CC1=O)C(=C)C	150.22	unknown	https://doi.org/10.1007/BF00579758
Carvone, (+/-)-	7439	Click to see CC1=CCC(CC1=O)C(=C)C	150.22	unknown	https://doi.org/10.1007/BF00579758
cis-p-Mentha-1(7),8-dien-2-ol	6429040	Click to see CC(=C)C1CCC(=C)C(C1)O	152.23	unknown	https://doi.org/10.1007/BF00579758
trans-1(7),8-p-Menthadien-2-ol	6428442	Click to see CC(=C)C1CCC(=C)C(C1)O	152.23	unknown	https://doi.org/10.1007/BF00579758
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Calamenene	11298625	Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C	202.33	unknown	https://doi.org/10.1007/BF00579758
(+)-delta-Cadinene	441005	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1007/BF00579758
(1R,4R,8S)-1-methyl-7-methylidene-4-propan-2-yl-11-oxabicyclo[6.2.1]undecan-3-one	163041439	Click to see CC(C)C1CCC(=C)C2CCC(O2)(CC1=O)C	236.35	unknown	https://doi.org/10.1007/BF00629824
(1S,3S,5R,6R,7S,10R)-3,7-dimethyl-10-propan-2-yltricyclo[4.4.0.01,5]decan-7-ol	162885712	Click to see CC1CC2C3C2(C1)C(CCC3(C)O)C(C)C	222.37	unknown	https://doi.org/10.1007/BF00565890
(E)-beta-farnesene	10407	Click to see CC(=CCCC(=CCCC(=C)C=C)C)C	204.35	unknown	https://doi.org/10.1007/BF00579758
1-Methyl-7-methylidene-4-propan-2-yl-11-oxabicyclo[6.2.1]undecan-3-one	101600415	Click to see CC(C)C1CCC(=C)C2CCC(O2)(CC1=O)C	236.35	unknown	https://doi.org/10.1007/BF00629824
1,4,8-Cycloundecatriene, 2,6,6,9-tetramethyl-, (1E,4E,8E)-	23204	Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C	204.35	unknown	https://doi.org/10.1007/BF00579758 https://doi.org/10.1002/JPS.3080230706
1,6-Dimethyl-4-isopropyltetralin	10224	Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C	202.33	unknown	https://doi.org/10.1007/BF00579758
2,6,6,9-Tetramethyl-cycloundeca-1,4,8-triene	6508206	Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C	204.35	unknown	https://doi.org/10.1002/JPS.3080230706
3,7-Dimethyl-10-propan-2-yltricyclo[4.4.0.01,5]decan-7-ol	162885711	Click to see CC1CC2C3C2(C1)C(CCC3(C)O)C(C)C	222.37	unknown	https://doi.org/10.1007/BF00565890
beta-Farnesene	5281517	Click to see CC(=CCCC(=CCCC(=C)C=C)C)C	204.35	unknown	https://doi.org/10.1007/BF00579758
Cadina-1(10),4-diene	10223	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1007/BF00579758
Humulene	5281520	Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C	204.35	unknown	https://doi.org/10.1007/BF00579758
Valerenal	6440942	Click to see CC1CCC(C2=C(CCC12)C)C=C(C)C=O	218.33	unknown	https://doi.org/10.1007/BF02276130
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(-)-Alloaromadendrene	10899740	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	https://doi.org/10.1007/BF00579758
(1aR,4R,4aS,7S,7aS,7bR)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol	42433470	Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O	222.37	unknown	https://doi.org/10.1246/NIKKASHI1921.64.1041 https://doi.org/10.1007/BF00579758
(1aR,7S,7aR,7bR)-1,1,4,7-tetramethyl-1a,2,3,5,6,7,7a,7b-octahydrocyclopropa[e]azulene	124540680	Click to see CC1CCC2=C(CCC3C(C12)C3(C)C)C	204.35	unknown	https://doi.org/10.1007/BF00629824
(1aS,4R,4aR,7bR)-1,1,4,7-tetramethyl-2,3,4,4a,5,7b-hexahydro-1aH-cyclopropa[e]azulen-6-one	163030918	Click to see CC1CCC2C(C2(C)C)C3=C(C(=O)CC13)C	218.33	unknown	https://doi.org/10.1007/BF01134621
1,1,4,7-Tetramethyl-1a,2,3,5,6,7,7a,7b-octahydrocyclopropa[e]azulene	89532	Click to see CC1CCC2=C(CCC3C(C12)C3(C)C)C	204.35	unknown	https://doi.org/10.1007/BF00629824
1,1,4,7-tetramethyl-2,3,4,4a,5,7b-hexahydro-1aH-cyclopropa[e]azulen-6-one	12305388	Click to see CC1CCC2C(C2(C)C)C3=C(C(=O)CC13)C	218.33	unknown	https://doi.org/10.1007/BF01134621
Alloaromadendren	91746537	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	https://doi.org/10.1007/BF00566074
Aromadendrene	91354	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	https://doi.org/10.1007/BF00579758
Cyclocolorenone	160491	Click to see CC1CCC2C(C2(C)C)C3=C(C(=O)CC13)C	218.33	unknown	https://doi.org/10.1007/BF01134621
Globulol	101716	Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O	222.37	unknown	https://doi.org/10.1007/BF00579758 https://doi.org/10.1246/NIKKASHI1921.64.1041
Ledum camphor	22297324	Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O	222.37	unknown	https://doi.org/10.1007/BF02276130 https://doi.org/10.1007/BF00937609 https://doi.org/10.1007/BF01134621 https://doi.org/10.1007/BF00565890
Palustrol	110745	Click to see CC1CCC2(C1C3C(C3(C)C)CCC2C)O	222.37	unknown	https://doi.org/10.1007/BF02276130 https://doi.org/10.1007/BF00579758 https://doi.org/10.1007/BF00937609 https://doi.org/10.1007/BF01134621 https://doi.org/10.1007/BF00566074 https://doi.org/10.1007/BF00565890
Palustrol (Ledum)	9794494	Click to see CC1CCC2(C1C3C(C3(C)C)CCC2C)O	222.37	unknown	https://doi.org/10.1007/BF00579758
Viridiflorene	10910653	Click to see CC1CCC2=C(CCC3C(C12)C3(C)C)C	204.35	unknown	https://doi.org/10.1007/BF02276130 https://doi.org/10.1007/BF00629824
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2R,4aS,6aS,6bR,8aR,10S,12aR,12bR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylic acid	7163172	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1007/BF00638770
(3S,4aR,6aR,6bS,8aS,11R,12S,12aR,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol	162977496	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)CO	442.70	unknown	https://doi.org/10.1007/BF00638770
(3S,4aR,6aS,6aR,8aR,12aS,14aR,14bR)-4,4,6a,8a,11,11,12a,14b-octamethyl-1,2,3,4a,5,6,6a,8,9,10,12,13,14,14a-tetradecahydropicen-3-ol	163034523	Click to see CC1(CCC2(CC=C3C(C2(C1)C)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C	426.70	unknown	https://doi.org/10.1007/BF00638770
4,4,6a,8a,11,11,12a,14b-Octamethyl-1,2,3,4a,5,6,6a,8,9,10,12,13,14,14a-tetradecahydropicen-3-ol	163034522	Click to see CC1(CCC2(CC=C3C(C2(C1)C)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C	426.70	unknown	https://doi.org/10.1007/BF00638770
beta-Ursolic acid	220774	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1007/BF00638770
Urs-12-ene-3,28-diol, (3beta)-	3266408	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)CO	442.70	unknown	https://doi.org/10.1007/BF00638770
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9S,10R,13R,14S,17S)-17-[(2R,5S)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	1738061	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1007/BF00638770
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1007/BF00638770
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
[(3R)-7-methylocta-1,6-dien-3-yl] acetate	163035683	Click to see CC(=CCCC(C=C)OC(=O)C)C	182.26	unknown	https://doi.org/10.1007/BF00579758
7-Methylocta-1,6-dien-3-yl acetate	101720995	Click to see CC(=CCCC(C=C)OC(=O)C)C	182.26	unknown	https://doi.org/10.1007/BF00579758
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
2-Methyl-6-methylideneocta-3,7-dien-2-ol	81478	Click to see CC(C)(C=CCC(=C)C=C)O	152.23	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.27-0551
3,7-Octadien-2-ol, 2-methyl-6-methylene-, (E)-	5363351	Click to see CC(C)(C=CCC(=C)C=C)O	152.23	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.27-0551
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Alpha-branched alpha,beta-unsaturated ketones
2-Methyl-6-methylene-1,7-octadien-3-one	93231	Click to see CC(=C)C(=O)CCC(=C)C=C	150.22	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.27-0551
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(1S,5R)-5-propan-2-ylbicyclo[3.1.0]hex-3-en-2-one	21626600	Click to see CC(C)C12CC1C(=O)C=C2	136.19	unknown	https://doi.org/10.1007/BF00601281
Dehydrosabinaketone	527426	Click to see CC(C)C12CC1C(=O)C=C2	136.19	unknown	https://doi.org/10.1007/BF00601281
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
(1S,4S,5S)-1-methyl-4-propan-2-ylbicyclo[3.1.0]hexan-2-one	130914701	Click to see CC(C)C1CC(=O)C2(C1C2)C	152.23	unknown	https://doi.org/10.1007/BF00601281
4-Isopropyl-1-methylbicyclo[3.1.0]hexan-2-one	14755547	Click to see CC(C)C1CC(=O)C2(C1C2)C	152.23	unknown	https://doi.org/10.1007/BF00601281
> Organoheterocyclic compounds / Benzofurans
(3aR,7aR)-6-methyl-3-methylidene-3a,4,5,7a-tetrahydro-1-benzofuran	162908127	Click to see CC1=CC2C(CC1)C(=C)CO2	150.22	unknown	https://doi.org/10.1007/BF00629824
3,9-Oxy-mentha-1,8(10)-diene	22216621	Click to see CC1=CC2C(CC1)C(=C)CO2	150.22	unknown	https://doi.org/10.1007/BF00629824
> Organoheterocyclic compounds / Dioxanes / 1,2-dioxanes
Ascaridole	10545	Click to see CC(C)C12CCC(C=C1)(OO2)C	168.23	unknown	https://doi.org/10.3987/S-1978-01-0029
cis-Isoascaridole	6430795	Click to see CC(C)C12CCC(C=C1)(OO2)C	168.23	unknown	https://doi.org/10.3987/S-1978-01-0029
> Organoheterocyclic compounds / Heteroaromatic compounds
2-Methyl-5-(fur-3-yl)-pent-1-en-3-ol	557594	Click to see CC(=C)C(CCC1=COC=C1)O	166.22	unknown	https://doi.org/10.1007/BF00566074
> Organoheterocyclic compounds / Oxepanes
Carvenone oxide	549742	Click to see CC1CCC2(C(C1=O)O2)C(C)C	168.23	unknown	https://doi.org/10.3987/S-1978-01-0029
cis-Carvenone oxide	6430794	Click to see CC1CCC2(C(C1=O)O2)C(C)C	168.23	unknown	https://doi.org/10.3987/S-1978-01-0029
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
(3R)-3-hydroxy-3-methyl-5-oxo-5-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(7-hydroxy-2-oxochromen-6-yl)oxyoxan-2-yl]methoxy]pentanoic acid	162986063	Click to see CC(CC(=O)O)(CC(=O)OCC1C(C(C(C(O1)OC2=C(C=C3C(=C2)C=CC(=O)O3)O)O)O)O)O	484.40	unknown	https://doi.org/10.1016/0031-9422(90)80221-2
(3S)-3-hydroxy-3-methyl-5-oxo-5-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(7-hydroxy-2-oxochromen-6-yl)oxyoxan-2-yl]methoxy]pentanoic acid	162986066	Click to see CC(CC(=O)O)(CC(=O)OCC1C(C(C(C(O1)OC2=C(C=C3C(=C2)C=CC(=O)O3)O)O)O)O)O	484.40	unknown	https://doi.org/10.1016/0031-9422(90)80221-2
2H-1-Benzopyran-2-one, 6-(beta-D-glucopyranosyloxy)-7-hydroxy-	5351506	Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O	340.28	unknown	https://doi.org/10.1016/0031-9422(90)80221-2
3-Hydroxy-3-methyl-5-oxo-5-[[3,4,5-trihydroxy-6-(7-hydroxy-2-oxochromen-6-yl)oxyoxan-2-yl]methoxy]pentanoic acid	14704512	Click to see CC(CC(=O)O)(CC(=O)OCC1C(C(C(C(O1)OC2=C(C=C3C(=C2)C=CC(=O)O3)O)O)O)O)O	484.40	unknown	https://doi.org/10.1016/0031-9422(90)80221-2
7-hydroxy-6-methoxy-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one	5281418	Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)O	370.31	unknown	https://doi.org/10.1016/0031-9422(90)80221-2
Esculin	5281417	Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O	340.28	unknown	https://doi.org/10.1016/0031-9422(90)80221-2
Fraxin	5273568	Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)O	370.31	unknown	https://doi.org/10.1016/0031-9422(90)80221-2
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin	5281416	Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O	178.14	unknown	https://doi.org/10.1002/CHIN.200322269
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7,8-dihydroxycoumarins
Fraxetin	5273569	Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)O)O	208.17	unknown	https://doi.org/10.1007/BF00638770
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin	5280460	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O	192.17	unknown	https://doi.org/10.1002/CHIN.200322269
Umbelliferone	5281426	Click to see C1=CC(=CC2=C1C=CC(=O)O2)O	162.14	unknown	https://doi.org/10.1002/CHIN.200322269
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	https://doi.org/10.1007/BF00638770
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	5378597	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1007/BF00638770
Hyperoside	5281643	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1007/BF00638770
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Myricetin 3,7,3',5'-tetramethyl ether	44259713	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C(=C3)OC)O)OC)O	374.30	unknown	https://doi.org/10.1007/BF00638770
Pachypodol	5281677	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)OC)O	344.30	unknown	https://doi.org/10.1007/BF00638770

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Rhododendron groenlandicum

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